Intervertebral fusion device with bone graft, cervical

FDA registration

Acero Precision·1 product·🇺🇸 United States

Altus Spine Cervical Interbody Fusion System

FDA registration

ALTUS PARTNERS·1 product·🇺🇸 United States

Altus Spine Cervical Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

SYNFIX-LR SPACER; K072253

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

Echo Blaster

FDA registration

TELEMED·2 products·🇱🇹 Lithuania

Jabil Switzerland Manufacturing GmbH (Bettlach)

FDA registration

Jabil Switzerland Manufacturing GmbH (Bettlach)·1 product·🇨🇭 Switzerland

Jabil Switzerland Manufacturing GmbH (Grenchen)

FDA registration

Jabil Switzerland Manufacturing GmbH (Grenchen)·1 product·🇨🇭 Switzerland

Jabil Inc. (Brandywine)

FDA registration

Jabil Inc. (Brandywine)·1 product·🇺🇸 United States

SYNFIX-LR SPACER

FDA registration

SYNTHES GMBH·1 product·🇨🇭 Switzerland

Jabil Inc. (Monument)

FDA registration

Jabil Inc. (Monument)·1 product·🇺🇸 United States

Synergy Health Daniken AG

FDA registration

Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

SYNFIX-LR SPACER

FDA registration

Synthes GMBH·1 product·🇨🇭 Switzerland

SYNFIX-LR SPACER

FDA registration

Synthes (USA) Products LLC·1 product·🇺🇸 United States

Technical Services for Electronics, Inc.

FDA registration

Technical Services for Electronics, Inc.·1 product·🇹🇼 Taiwan

ECHO BLASTER

FDA 510(k)

FDA Class 2 ·Radiology

SYNFIX-LR SPACER

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical

Intervertebral Fusion Device With Integrated Fixation, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar

System, Imaging, Pulsed Echo, Ultrasonic

FDA classification

FDA Class 2 ·System, Imaging, Pulsed Echo, Ultrasonic